The p47-phox gene has a pseudogene carrying the most common mutation for p47-phox deficient chronic granulomatous disease.

被引：0

作者：

Gorlach, A

Roesler, J

Hopkins, PJ

Christensen, BL

Lee, P

Green, ED

Chanock, SJ

Curnutte, JT

机构：

[1] SCRIPPS RES INST, LA JOLLA, CA USA

[2] GENENTECH INC, S SAN FRANCISCO, CA 94080 USA

[3] NCI, PEDIAT BRANCH, BETHESDA, MD 20892 USA

[4] NIH, NATL CTR HUMAN GENOME RES, BETHESDA, MD 20892 USA

来源：

BLOOD | 1995年 / 86卷 / 10期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1027 / 1027

页数：1

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[20] NEUTROPHIL NICOTINAMIDE ADENINE-DINUCLEOTIDE PHOSPHATE OXIDASE ASSEMBLY - TRANSLOCATION OF P47-PHOX AND P67-PHOX REQUIRES INTERACTION BETWEEN P47-PHOX AND CYTOCHROME-B558 [J].

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